Medical use for tachykinin antagonists

ABSTRACT

The present invention relates to the use of certain tachykinin antagonists, including substance P antagonists and other neurokinin antagonists, in the treatment of emesis.

The present invention relates to the use of certain tachykinin antagonists, including substance P antagonists and other neurokinin antagonists, in the treatment of emesis.

Tachykinin antagonists are known to be useful in the treatment of a variety of disorders including pain, inflammatory diseases, allergic disorders, CNS disorders, skin disorders, cough and gastrointestinal disorders such as ulcerative colitis and Crohn's disease.

It has now been found that tachykinin antagonists, including substance P antagonists and other neurokinin antagonists, are useful in the treatment of emesis. Our co-pending European Patent Application No. 92202831 (Publication No. 0533280) relates to the use of tachykinin antagonists in the treatment of emesis.

The use of the tachykinin antagonists, including substance P antagonists and other neurokinin antagonists, specifically disclosed in co-pending European Patent Application No. 92202831 in the treatment of emesis is not included within the scope of the present invention.

The invention accordingly provides, in a first aspect, the novel use of the tachykinin antagonists, including substance P antagonists and other neurokinin antagonists, generically and specifically disclosed in published European Patent Application Nos. 512901, 512902, 514273, 514275, 517589, 520555, 522808, 528495, 532456 and published PCT Patent Application Nos. 92/15585, 92/17449, 92/20661, 92/20676, 92/21677, 92/22569, 93/00331, 93/01159, 93/01160, 93/01165, 93/01169 and 93/01170, which disclosures are incorporated herein by reference, in the treatment of emesis.

There is also provided as a further aspect of the invention the use of the tachykinin antagonists, including substance P antagonists and other neurokinin antagonists, generically and specifically disclosed in the above referenced patent specifications in the preparation of a medicament for use in the treatment of emesis.

In an alternative or further aspect there is provided a method for the treatment of a mammal, including man, suffering from or susceptible to emesis, comprising administration of an effective amount of a tachykinin antagonist, including substance P antagonists and other neurokinin antagonists, generically or specifically disclosed in the above referenced patent specifications.

It will be appreciated that reference to treatment is intended to include prophylaxis as well as the alleviation of established symptoms.

Tachykinin antagonists, including substance P antagonists and other neurokinin antagonists, disclosed in the above referenced patent specifications have been shown to have anti-emetic activity as indicated by for example their ability to inhibit cisplatin- or radiation-induced emesis in the ferret.

The treatment of emesis mentioned hereinbefore includes the treatment of nausea, retching and vomiting. Emesis includes acute emesis, delayed emesis and anticipatory emesis. Tachykinin antagonists, including substance P antagonists and other neurokinin antagonists, are useful in the treatment of emesis however induced. For example, emesis may be induced by drugs such as cancer chemotherapeutic agents such as alkylating agents, e.g. cyclophosphamide, carmustine, lomustine and chlorambucil; cytotoxic antibiotics, e.g. dactinomycin, doxorubicin, mitomycin-C and bleomycin; anti-metabolites, e.g. cytarabine, methotrexate and 5-fluorouracil; vinca alkaloids, e.g. etoposide, vinblastine and vincristine; and others such as cisplatin, dacarbazine, procarbazine and hydroxyurea; and combinations thereof; radiation sickness; radiation therapy, e.g. irradiation of the thorax or abdomen, such as in the treatment of cancer; poisons; toxins such as toxins caused by metabolic disorders or by infection, e.g. gastritis; pregnancy; vestibular disorders, such as motion sickness and vertigo; post-operative sickness; gastrointestinal obstruction; reduced gastrointestinal motility; visceral pain, e.g. myocardial infarction or peritonitis; migraine; increased intercranial pressure; decreased intercranial pressure (e.g. altitude sickness); and opioid analgesics, such as morphine.

Tachykinin antagonists acting at NK₁ receptors have been found to be particularly useful in the treatment of emesis.

In a preferred aspect therefore the invention provides the use of an NK₁ receptor antagonist generically or specifically disclosed in the above referenced patent specifications in the treatment of emesis.

Particularly preferred tachykinin antagonists for use in the present invention include those generically and specifically disclosed in:

EP512901, i.e. compounds of the formula ##STR1## wherein Y represents a group Cy--N or Cy--CH₂ --N wherein

Cy represents phenyl optionally substituted by one or more groups, which may be the same or different, selected from halogen, hydroxy, C₁₋₄ alkoxy, C₁₋₄ alkyl, trifluoromethyl; C₃₋₇ cycloalkyl; pyrimidinyl; or pyridyl;

or Y represents a group Ar--(CH₂)_(x) C(X)-- wherein

Ar represents phenyl optionally substituted by one or more groups, which may be the same or different, selected from hydrogen, halogen, hydroxy, C₁₋₄ alkoxy, trifluoromethyl, C₁₋₄ alkyl; pyridyl; or thienyl;

x is zero or 1;

X represents hydrogen, hydroxy, C₁₋₄ alkoxy, C₁₋₄ acyloxy, carboxy, C₁₋₄ alkoxycarbonyl, cyano, a group N(X₁)₂ wherein X₁ represents independently hydrogen, C₁₋₄ alkyl, hydroxy C₁₋₄ alkyl, C₁₋₄ acyl or --(X₁)₂ represents, together with the nitrogen atom to which it is attached, a heterocycle selected from pyrrolidine, piperidine or morpholine; a group --S--X₂ wherein X₂ represents hydrogen or C₁₋₄ alkyl; or X forms a double bond with an adjacent carbon atom;

m is 2 or 3;

Ar¹ represents phenyl optionally substituted by one or more groups, which may be the same or different, selected from halogen, preferably chlorine or fluorine, trifluoromethyl, C₁₋₄ alkoxy, C₁₋₄ alkyl; thienyl; benzothienyl; naphthyl; or indolyl;

n is zero 1, 2 or 3;

p is 1 or 2 provided that p is 2 when n is 1 and Q represents two hydrogen atoms;

Q represents oxygen or two hydrogen atoms;

T represents a group selected from C(O) and --CH₂ --;

q is zero, 1, 2 or 3;

Z represents phenyl optionally substituted by one or more groups selected from halogen, more particularly chlorine or fluorine, trifluoromethyl, C₁₋₄ alkyl, hydroxyl, C₁₋₄ alkoxy; naphthyl optionally substituted by one or more groups selected from halogen, trifluoromethyl, C₁₋₄ alkyl, hydroxyl; pyridyl; thienyl; indolyl; quinolyl; benzothienyl; imidazolyl; or in addition when T represents C(O), --(CH₂)_(q) --Z may also represent a benzyl group substituted on the --CH-- by hydroxy, C₁₋₄ alkoxy or C₁₋₄ alkyl group and optionally substituted on the aromatic ring by halogen, more particularly chlorine or fluorine, trifluoromethyl, C₁₋₄ alkyl, hydroxy, C₁₋₄ alkoxy; or an optionally substituted mono-, bi- or tricyclic aromatic or heteroaromatic group; and salts thereof with mineral or organic acids, or, where Y represents Ar--(CH₂)_(x) --C(X)--, quarternary ammonium salts or N-oxides formed with the piperidine nitrogen atom (b). EP 512902, i.e. compounds of the formula ##STR2## wherein Ar¹ represents phenyl optionally substituted by halogen, C₁₋₃ alkyl, trifluoromethyl, C₁₋₃ alkoxy or hydroxy; thienyl, pyridyl or naphthyl optionally substituted by halogen; indolyl; or benzothienyl;

R represents hydrogen, methyl or (CH₂)_(n) L;

n represents 2 to 6;

L represents hydrogen or amino;

Z and Z¹ represent hydrogen, M or OM;

M represents hydrogen, C₁₋₆ alkyl, a-hydroxybenzyl, a-(C₁₋₃ alkyl)benzyl, phenylC₁₋₃ alkyl (optionally ring substituted by halogen, hydroxy, C₁₋₄ alkoxy or C₁₋₄ alkyl), pyridylC₁₋₃ alkyl, naphthylC₁₋₃ alkyl, pyridylthioC₁₋₃ alkyl, styryl, 1 -methyl-2-imidiazolylthioC₁₋₃ alkyl, 1-oxo-3-phenyl-2-indanyl, or optionally substituted aryl or heteroaryl;

T¹ =a bond, CH₂ or CO;

T=CO or C(W)NH;

W=O or S;

with the proviso that (a) T¹ is not a bond when Z¹ is hydrogen or OM; and (b) T is not C(W)NH when Z is hydrogen or OM;

and acid addition and quarternary ammonium salts thereof.

EP 514273, i.e. compounds of the formula ##STR3## wherein R each represent hydrogen or together form a bond;

R¹ are the same and represent phenyl optionally substituted in the 2- or 3-position by halogen or methyl;

X represents O or NH;

R₁ represents phenyl optionally substituted by one or more halogen, hydroxy, alkyl (optionally substituted by halogen, amino, alkylamino or dialkylamino), alkyloxy or alkylthio (both optionally substituted by hydroxy, amino, alkylamino, dialkylamino (optionally substituted by phenyl, hydroxy or amino) or dialkylamino where the alkyl groups form, together with the nitrogen atom to which they are attached, a 5- or 6-membered heterocyclic ring which may contain a further heteroatom selected from oxygen, sulfur or nitrogen, optionally substituted by alkyl, hydroxy or hydroxyalkyl), or substituted by amino, alkylamino, dialkylamino (where the alkyl groups, together with the nitrogen atom to which they are attached, may form a heterocycle as defined above), or R₁ represents cyclohexadienyl, naphthyl, or a 5-9-membered mono- or polyheterocyclic ring, optionally saturated, and containing one more heteroatoms selected from oxygen, nitrogen and sulfur;

R₂ represents hydrogen, halogen, hydroxy, alkyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, alkyloxy, alkylthio, acyloxy, carboxy, alkyloxycarbonyl, dialkylaminoalkyloxycarbonyl, benzyloxycarbonyl, amino, acylamino, or alkyloxycarbonylamino;

R₃ represents halogen or hydroxy;

R₄ represents hydrogen; or R₃ and R₄ are both halogen; and salts thereof.

EP 514275; i.e. compounds of the formula ##STR4## wherein X represents NH or an oxygen atom; R₁ represents phenyl optionally substituted by one or more groups selected from halogen, hydroxy, alkyl (optionally substituted by halogen, amino, alkylamino or dialkylamino), alkyloxy or alkylthio [optionally substituted by hydroxy, amino, alkylamino or dialkylamino (optionally substituted by phenyl, hydroxy or amino), or dialkylamino where the alkyl groups form, together with the nitrogen atom to which they are attached, a 5- or 6-membered heterocyclic ring optionally containing a further heteroatom selected from oxygen, sulphur or nitrogen, optionally substituted by alkyl, hydroxy or hydroxyalkyl], or substituted by amino, alkylamino, dialkylamino where the alkyl groups optionally form, together with the nitrogen atom to which they are attached, a heterocycle as defined above, or represent a cyclohexadienyl, naphthyl or a mono or polycylic, saturated or unsaturated, ring containing 5 to 9 carbon atoms and one or more heteroatoms selected from oxygen, nitrogen or sulphur;

R₂ represents hydrogen, halogen, hydroxy, alkyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, alkyloxy, alkylthio, acyloxy, carboxy, alkyloxycarbonyl, dialkylaminoalkyloxycarbonyl, benzyloxycarbonyl, amino, alkylamino or alkyloxycarbonylamino; n is an integer from zero to 2; and salts thereof.

EP 520555, i.e. compounds of the formula (E) or a salt or prodrug thereof ##STR5## wherein Q is the residue of an optionally substituted azabicyclic ring system;

X represents oxa or thia;

Y represents H or hydroxy;

R¹ represents phenyl or thienyl, either of which groups may be optionally substituted by halo, trifluoromethyl or C₁₋₃ alkoxy, or C₅₋₇ cycloalkyl;

R² represents benzyl which may be substituted in the benzyl ring by halo, trifluoromethyl or C₁₋₃ alkoxy, or C₅₋₇ cycloalkyl; and

R³, R⁴ and R⁵ independently represent H, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, --OR^(a), SCH₃, SOCH₃, SO₂ CH₃, --NR^(a) R^(b), --NR^(a) CO₂ R^(b), --NR^(a) CO₂ R^(b), --CO₂ R^(a) or --CONR^(a) R^(b) ; and

R^(a) and R^(b) independently represent H, C₁₋₆ alkyl, phenyl or trifluoromethyl.

EP 522808, i.e compounds of formula (F) or a salt or prodrug thereof ##STR6## wherein Q represents R⁹ CR¹⁰ R¹¹ or CH₂ R⁹ CR¹⁰ R¹¹ where R⁹ is H or hydroxy and R¹⁰ and R¹¹ each independently represent optionally substituted phenyl, optionally substituted benzyl, C₅₋₇ cycloalkyl or (C₅₋₇ cycloalkyl)methyl;

R¹ and R² independently represent H; C₁₋₆ alkyl optionally substituted by hydroxy, cyano, COR^(a), COOR^(a), CONR^(a) R^(b), COC₁₋₆ alkylNR^(a) R^(b), CONR¹² C₁₋₆ alkylOR^(a), CONR¹² C₁₋₆ alkylCONR^(a) R^(b) or NR^(a) R^(b) (where R^(a) and R^(b) each independently represent H, C₁₋₆ alkyl, phenyl (optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl), phenyl(C₁₋₄ alkyl) (optionally substituted in the phenyl ring by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl) or R^(a) and R^(b) together form a chain (CH₂)_(p) optionally substituted by oxo where p is 4 or 5 and where one methylene group may optionally be replaced by an oxygen atom or a group NR^(x), where R^(x) is H or C₁₋₆ alkyl, and R¹² represents H, C₁₋₆ alkyl, phenyl (optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl) or phenyl (C₁₋₄ alkyl) (optionally substituted in the phenyl ring by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl); phenyl(C₁₋₄ alkyl) (optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl in the phenyl ring); C₂₋₆ alkenyl; C₂₋₆ alkynyl; COR^(a) ; COOR^(a), COC₁₋₆ alkylhalo; COC₁₋₆ alkylNR^(a) R^(b) ; CONR¹² C₁₋₆ alkylCONR^(a) R^(b) ; CONR^(a) R^(b) or SO₂ R^(a) ; (where R^(a), R^(b) and R¹² are as previously defined) or R¹ and R² together form a chain (CH₂)_(q) optionally substituted by oxo where q is 4 or 5 and where one methylene group may optionally be replaced by an oxygen atom or a group NR^(x), where R^(x) is H or C₁₋₆ alkyl;

R³ represents H, C₁₋₆ alkyl or C₂₋₆ alkenyl;

R⁴ represents C₁₋₃ alkyl substituted by a phenyl group which may itself optionally be substituted by one or more of C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, SR^(c), SOR^(c), SO₂ R^(c), OR^(c), NR^(c) R^(d), NR^(c) COR^(d), NR^(c) COOR^(d), COOR^(c) and CONR^(c) R^(d), where R^(c) and R^(d) independently represent H, C₁₋₆ alkyl, phenyl or trifluoromethyl;

X and Y each represent H, or X and Y together represent a group ═O; and

Z represents O, S or NR⁷, where R⁷ represents H or C₁₋₆ alkyl; with the exception of

DL-diphenylalanine benzyl ester;

2-benzamido-3,3-diphenylpropanoyl benzamide; and

2-benzamido-3,4-diphenyl-butanoyl benzamide.

For example 2-ammonium-1-((3,5-bis(trifluoromethyl)phenyl)methyloxy)-3,3-diphenylpropane--Compound 1; and salts and prodrugs thereof.

EP 528495, i.e. compounds of formula (G) or a salt or prodrug thereof ##STR7## wherein n is 1, 2, or 3 and where any carbon atom of (CH₂)_(n) may be substituted by R⁴ and/or R⁵ ;

X represents O or S;

R¹ represents phenyl optionally substituted by 1, 2 or 3 groups selected from C₁₋₆ alkyl, C₂₋₆ alkenyl; C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, --OR^(a), SR^(a), SOR^(a), SO₂ R^(a), --NR^(a) R^(b), --NR^(a) COR^(b), --NR^(a) CO₂ R^(b), CO₂ R^(a) or --CONR^(a) R^(b) ;

R² represents aryl selected from phenyl and naphthyl; heteroaryl selected from indazolyl, thienyl, furyl, pyridyl, thiazolyl, tetrazolyl and quinolyl; benzhydryl; or benzyl; wherein each aryl or heteroaryl moiety may be substituted by C₁₋₆ alkyl, C₁₋₆ alkoxy, halo or trifluoromethyl;

R⁴ and R⁵ each independently represent H, halo, CH₂ OR⁹, C₁₋₆ alkyl, oxo, CO₂ R¹⁰ or CONR¹⁰ R¹¹ ;

R⁸ represents H, COR⁹, CO₂ R¹⁰, COCONR¹⁰ R¹¹, COCO₂ R¹⁰ or C₁₋₆ alkyl optionally substituted by a group selected from (CO₂ R¹⁰, CONR¹⁰ R¹¹, hydroxy, cyano, COR⁹, NR¹⁰ R¹¹, C(NOH)NR¹⁰ R¹¹, CONHphenyl-(C₁₋₄ alkyl), COCO₂ R¹⁰, COCONR¹⁰ R¹¹ and phenyl optionally substituted by one or more substituents selected from C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl);

R^(a) and R^(b) each independently represent H, C₁₋₆ alkyl, phenyl or trifluoromethyl;

R⁹ represents H, C₁₋₆ alkyl or phenyl; and

R¹⁰ and R¹¹ each independently represent H or C₁₋₆ alkyl.

For example cis-3-((3,5-dimethylphenyl)methyloxy)-2-phenylpiperidine--Compound 5; and salts (e.g. the hydrochloride salt) and prodrugs thereof.

WO 92/22569, i.e. compounds of formula ##STR8## wherein R¹ is lower alkyl, aryl, ar(lower)alkyl, arylamino, pyridyl, pyrrolyl, pyrazolopyridyl, quinolyl, or a group of the formula ##STR9## wherein the symbol of a line and dotted line is a single bond or a double bond,

X is CH or N, and

Z is O, S or NH,

each of which may have suitable substituent(s);

R² is hydrogen or lower alkyl;

R³ is hydrogen or suitable substituent;

R⁴ is lower alkyl which may have suitable substituent(s), and

R⁵ is ar(lower)alkyl which may have suitable substituent(s) or pyridyl(lower)alkyl, or

R⁴ and R⁵ are linked together to form benzene-condensed lower alkylene;

A is an amino acid residue which may have suitable substituent(s); and

Y is bond, lower alkylene, lower alkenylene or lower alkylimino, provided that when

R¹ is aryl, or a group of the formula: ##STR10## wherein X is as defined above, and Z is O or N--R⁶ _(a), in which R⁶ _(a) is hydrogen or lower alkyl,

R² is hydrogen,

R⁴ is lower alkyl which may have suitable substituent(s),

R⁶ is ar(lower)alkyl which may have suitable substituent(s),

A is group of the formula: ##STR11## wherein R⁷ is hydroxy or lower alkoxy, and Y is bond or lower alkenylene, then

R³ is suitable substituent.

WO 92/15585, i.e. compounds of the formula ##STR12## wherein R¹, R², R³, R⁴, R⁵, and R⁶ are each independently selected from hydrogen, fluorine, chlorine, bromine, trifluoromethyl, alkyl having from one to three carbon atoms, alkoxy having from one to three carbon atoms, carboxy, alkoxycarbonyl having from one to three carbon atoms in the alkoxy moiety, and benzyloxycarbonyl; and the pharmaceutically acceptable salts of such compounds.

WO 92/17449, i.e. compounds of the formula ##STR13## wherein R¹ is aryl selected from indanyl, phenyl and naphthyl; heteroaryl selected from thienyl, furyl, pyridyl and quinolyl; and cycloalkyl having 3 to 7 carbon atoms, wherein one of said carbon atoms may optionally be replaced by nitrogen, oxygen or sulfur; wherein each of said aryl and heteroaryl groups may optionally be substituted with one or more substituents, and said (C₃ -C₇)cycloalkyl may optionally be substituted with one or two substituents, said substituents being independently selected from chloro, fluoro, bromo, iodo, nitro, (C₁ -C₁₀)alkyl optionally substituted from one to three fluoro groups, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluoro groups, amino, (C₁ -C₁₀)alkyl-S--, (C₁ -C₁₀)alkyl-S(O)--, (C₁ -C₁₀)alkyl-SO₂ --, phenyl, phenoxy, (C₁ -C₁₀)alkyl-SO₂ NH--, (C₁ -C₁₀)alkyl-SO₂ NH-(C₁ -C₁₀)alkyl-, (C₁ -C₁₀)alkylamino-di(C₁ -C₁₀)alkyl-, cyano, hydroxy, cycloalkoxy having 3 to 7 carbon atoms, (C₁ -C₆)alkylamino, (C₁ -C₆)dialkylamino, HC(O)NH-- and (C₁ -C₁₀)alkyl-C(O)--NH--, wherein the nitrogen atoms of said amino and (C₁ -C₆)alkylamino groups may optionally be protected with an appropriate protecting group; and R² is thienyl, benzhydryl, naphthyl or phenyl optionally substituted with from one to three substituents independently selected from chloro, bromo, fluoro, iodo, cycloalkoxy having 3 to 7 carbon atoms, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluoro groups and (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluoro groups.

For example

(2S,3S)-3-(2-Methoxy-5-methylmercaptobenzylamino)-2-phenylpiperidine--Compound 2.

WO 92/20661, i.e. compounds of the formula ##STR14## or a pharmaceutically acceptable salt thereof wherein: R^(1a) is

1) H,

2) C₁₋₈ alkyl,

3) phenyl, either unsubstituted or substituted with one or two substituents selected from:

a) --C₁₋₄ alkyl,

b) -halo,

e) --OH,

d) --CF₃,

e) --NH₂,

f) --NH(C₁₋₄ alkyl),

g) --N(C₁₋₄ alkyl)₂,

h) --CO₂ H,

i) --CO₂ (C₁₋₄ alkyl), and

j) --C₁₋₄ alkoxy; or

4) C₁₋₄ alkyl-phenyl, wherein the phenyl is either unsubstituted or substituted with one or two substituents selected from:

a) --C₁₋₄ alkyl,

b) -halo,

e) --OH,

d) --CF₃,

e) --NH₂,

f) --NH(C₁₋₄ alkyl),

g) --N(C₁₋₄ alkyl)₂,

h) --CO₂ H

i) --CO₂ (C₁₋₄ alkyl), and

j) --C₁₋₄ alkoxy;

R^(1b) is

1) R^(1a),

2) --C₃₋₇ cycloalkyl, or

3) --CH₂ --R^(1a) ;

R^(2a) and R^(2b) are independently phenyl, either unsubstituted or substituted with one or two substituents selected from:

1) --C₁₋₄ alkoxy,

2) -halo,

3) --OH,

4) --CF₃

5) --NH₂,

6) --N(C₁₋₄ alkyl),

7) --N(C₁₋₄ alkyl)₂,

8) --CO₂ H,

9) --CO₂ (C₁₋₄ alkyl), and

10) --C₁₋₆ alkyl, either unsubstituted or substituted with:

a) -halo,

b) --OH,

c) --CF₃,

d) --NH₂,

e) --NH(C₁₋₄ alkyl),

f) --N(C₁₋₄ alkyl)₂,

g) --CO₂ H,

h) --CO₂ (C₁₋₄ alkyl), and

i) --C₁₋₄ alkoxy,

j) --S(O)_(x) (C₁₋₄ alkyl) wherein x is 0, 1 or 2,

k) --C₃₋₇ cycloalkyl;

and the phenyl groups of R^(2a) and R^(2b) may be joined together at the ortho carbon atoms through a carbon-carbon single bond or C₁₋₃ alkylene to form a tricyclic group with the X² to which they are attached;

X¹ is --N, --CH or 0, and if X¹ is 0, R^(1a) is absent:

X² is --N or --CH;

R³ is

1) --C₁₋₄ alkyl,

2) --CO₂ R⁶,

3) --CH₂ OCOR⁶,

4) --CH₂ OH,

5) --CH₂ OR⁵,

6) --CH₂ S(O)_(x) R⁵,

7) --CH₂ OCONR⁵ R⁶,

8) --CH₂ CONR⁵ R⁶,

9) CONR⁵ R⁶,

10) --CO₂ R⁸,

11) --CH₂ CO₂ R⁶,

12) --CH₂ CO₂ R⁸,

13) --CONRSO₂ R⁹,

14) --CH₂ N(R⁶)CONR⁵ R⁶,

15) --CH₂ NH₂,

16) --CH₂ NH(C₁₋₄ alkyl), or

17) --CH₂ N(C₁₋₄ alkyl)₂ ; wherein

R⁵ is C₁₋₆ alkyl either unsubstituted or substituted with:

1) -halo,

2) --OH,

3) --CF₃

4) --NH₂,

5) --NH(C₁₋₄ alkyl),

6) --N(C₁₋₄ alkyl)₂,

7) --CO₂ H,

8) --CO₂ (C₁₋₄ alkyl),

9)--C₃₋₇ cycloalkyl, or

10) phenyl, either unsubstituted or substituted with

a) --C₁₋₄ alkyl,

b) -halo,

c) --OH,

d) --CF₃

e) --NH₂,

f) --NH(C₁₋₄ alkyl),

g) --N(C₁₋₄ alkyl)₂,

h) --CO₂ H, or

i) --CO₂ (C₁₋₄ alkyl);

R⁶ is --H or C₁₋₄ alkyl; or

R⁵ and R⁶ can be joined together to form with the nitrogen to which they are attached --N(CH₂ CH₂)₂ L; wherein L is:

i) a single bond,

ii) --OH₂ --,

iii) --O--,

iv) --S(O)_(p) --, or

v) --NR⁷ ;

R⁷ is

1) --H,

2) --C₁₋₆ alkyl, unsubstituted or substituted with --OH, --C₁₋₄ alkoxy or --N(C₁₋₄ alkyl)₂,

3) -aryl, or

4) --CH₂ -aryl;

R⁸ is

1) --H,

2) --CH(R⁷)OCOR¹⁰, wherein R¹⁰ is

a) --C₁₋₆ alkyl,

b) -aryl, or

c) --CH₂ -aryl,

3) --CH₂ -aryl,

R⁹ is

1) -aryl,

2) -heteroaryl,

3) --C₃₋₇ cycloalkyl,

4) polyfluoro-C₁₋₄ alkyl

5) --C₁₋₆ alkyl, either unsubstituted or substituted with

a) -aryl,

b) -heteroaryl,

c) OH,

d) --SH,

e) --C₁₋₄ alkyl,

f) --C₃₋₇ cycloalkyl,

g) --C₁₋₄ alkoxy

h) --C₁₋₄ alkylthio,

i) --CF₃,

j) -halo,

k) --NO₂,

l) --CO₂ R⁶,

m) --N(R⁶)₂, wherein the R⁶ groups are the same or different,

n) --NH-aryl,

o) --N(aryl)₂,

p) --PO₃ H,

q) --PO(OH)(OC₁₋₄ alkyl) or

r) --N(CH₂ CH₂)₂ L wherein L is as defined above, and

R⁴ is H or R³.

WO 92/20676, i.e. compounds of the formula ##STR15## wherein W is Y or X(CH₂)_(n) ; Y is optionally substituted (C₁ -C₆)alkyl, optionally substituted (C₂ -C₆)alkenyl or optionally substituted (C₃ -C₆)cycloalkyl;

X is optionally substituted (C₁ -C₆)alkoxy, CONR¹ R², CO₂ R¹, CHR¹ OR², CHR¹ NR² R³, COR¹, CONR¹ OR² or optionally substituted aryl, wherein said aryl is selected from phenyl, naphthyl, pyridyl, quinolyl, thienyl, furyl, phenoxyphenyl, oxazolyl, tetrazolyl, thiazolyl, imidazolyl and pyrazolyl; and n is an integer from zero to six;

Ar¹, Ar² and Ar³ are each, independently, optionally substituted aryl, wherein said aryl is selected from phenyl, naphthyl, pyridyl, quinolyl, thienyl, furyl, phenoxyphenyl, oxazolyl, tetrazolyl, thiazolyl, imidazolyl and pyrazolyl; and R¹, R² and R³ are independently selected from hydrogen, optionally substituted (C₁ -C₆)alkyl, optionally substituted (C₁ -C₆)alkoxy, optionally substituted (C₃ -C₈)cycloalkyl, optionally substituted aryl, wherein said aryl is selected from phenyl, naphthyl, pyridyl, quinolyl, thienyl, furyl, phenoxyphenyl, oxazolyl, tetrazolyl, thiazolyl, imidazolyl and pyrazolyl; and optionally substituted (C₁ -C₅)heterocyclic groups, wherein said heterocyclic groups are selected from pyrrolidino, piperidino, morpholino, piperazinyl and thiamorpholino;

and wherein the substituents on the foregoing substituted alkyl, alkenyl, cycloalkyl and alkoxy groups are independently selected from halo, nitro, amino, (C₁ -C₄)alkyl, (C₁ -C₄)alkoxy, trifluoromethyl and trifluoromethoxy;

and wherein the substituents on the foregoing substituted heterocyclic groups are attached to an oxygen or nitrogen atom on the ring and are independently selected from oxygen and (C₁ -C₄)alkyl;

and wherein the substituents on said substituted Ar¹ groups are independently selected from (C₁ -C₆)alkyl optionally substituted with from one to three halo groups. (C₁ -C₆)alkoxy optionally substituted from one to three halo groups, (C₁ -C₆)alkylsulfinyl, (C₂ -C₆)alkenyl, (C₁ -C₆)alkylthio, (C₁ -C₆)alkylsulfonyl, (C₁ -C₆)alkylsulfonylamino, and di-(C₁ -C₆)alkylamino wherein one or both of the alkyl groups may be optionally substituted with a (C₁ -C₆)alkylsulfonyl, or (C₁ -C₆)alkylsulfinyl group;

and wherein the substituents on said substituted Ar² and Ar³ groups are independently selected from (C₁ -C₄)alkyl, (C₁ -C₄)alkoxy, (C₁ -C₄)alkylthio, (C₁ -C₄)alkylsulfinyl, di-(C₁ -C₄)alkylamino, trifluoromethyl and trifluoromethoxy,

and wherein the substituents on said substituted (C₁ -C₅) heterocyclic groups are independently selected from oxygen and (C₁ -C₄)alkyl.

WO 92/21677, i.e. compounds of the formula ##STR16## wherein R¹ is methoxy and R² is independently selected from the group consisting of isopropyl, tert-butyl, methyl, ethyl and sec-butyl; and the pharmaceutically acceptable salts of such compounds.

WO 93/00331, i.e. compounds of the formula ##STR17## wherein X¹ is hydrogen, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms or (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms;

X² and X³ are independently selected from hydrogen, halo, nitro, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms, trifluoromethyl, hydroxy, phenyl, cyano, amino, (C₁ -C₆)-alkylamino, di-(C₁ -C₆)alkylamino, --C(O)--NH-(C₁ -C₆)-alkyl, (C₁ -C₆)alkyl-C(O)--NH-(C₁ -C₆)alkyl, hydroxy(C₁ -C₄)alkyl, (C₁ -C₄)alkoxy(C₁ -C₄)alkyl, --NHC(O)H and --NHC(O)-(C₁ -C₆)alkyl; and Q is a group of the formula ##STR18## wherein R¹ is a radical selected from furyl, thienyl, pyridyl, indolyl, biphenyl and phenyl optionally substituted with one or two substituents independently selected from halo, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms, carboxy, benzyloxycarbonyl and (C₁ -C₃)alkoxy-carbonyl;

R¹³ is selected from (C₃ -C₄) branched alkyl, (C₅ -C₆) branched alkenyl, (C₅ -C₇)cycloalkyl, and the radicals named in the definition of R¹ ;

R² is hydrogen or (C₁ -C₆)alkyl;

R³ is phenyl, biphenyl, naphthyl, pyridyl, benzhydryl, thienyl or furyl, and R³ may optionally be substituted with from one to three substituents independently selected from halo, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms and (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms;

Y is (CH₂)_(l) wherein l is an integer from one to three or Y is a group of the formula ##STR19## Z is oxygen, sulfur, amino, (C₁ -C₃)alkylamino or (CH₂)_(n) wherein n is zero, one or two;

o is two or three;

p is zero or one;

R⁴ is furyl, thienyl, pyridyl, indolyl, biphenyl, or phenyl optionally substituted with one or two substituents independently selected from halo, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms, carboxy, (C₁ -C₃)alkoxy-carbonyl and benzyloxycarbonyl;

R⁵ is thienyl, biphenyl or phenyl optionally substituted with one or two substituents independently selected from halo, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms and (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms;

each of the two dashed lines in formula (N) and the dashed line in formula (II) represent an optional double bond that may optionally exist when Q is a group of the formula (II);

X is (CH₂)_(q) wherein q is an integer from 1 to 6, and wherein any one of the carbon-carbon single bonds in said (CH₂)_(q) may optionally be replaced by a carbon-carbon double bond, and wherein any one of the carbon atoms of said (CH₂)_(q) may optionally be substituted with R⁸, and wherein any one of the carbon atoms of said (CH₂)_(q) may optionally be substituted with R⁹ ;

m is an integer from 0 to 8, and any one of the carbon-carbon single bonds of (CH₂)_(m) may optionally be replaced by a carbon-carbon double bond or a carbon-carbon triple bond, and any one of the carbon atoms of said (CH₂)_(m) may optionally be substituted with R¹¹ ;

R⁶ is a radical selected from hydrogen, (C₁ -C₆) straight or branched alkyl, (C₃ -C₇)cycloalkyl wherein one of the carbon atoms may optionally be replaced by nitrogen, oxygen or sulfur; aryl selected from biphenyl, phenyl, indanyl and naphthyl; heteroaryl selected from thienyl, furyl, pyridyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, triazolyl, tetrazolyl and quinolyl; phenyl (C₂ -C₆)alkyl, benzhydryl and benzyl, wherein each of said aryl and heteroaryl groups and the phenyl moieties of said benzyl, phenyl (C₂ -C₆)alkyl and benzhydryl may optionally be substituted with one or more substituents independently selected from halo, nitro, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms, amino, hydroxy-(C₁ -C₆)alkyl, (C₁ -C₆)alkoxy-(C₁ -C₆)alkyl, (C₁ -C₆)-alkylamino, (C₁ -C₆)alkyl-O--C(O)--, (C₁ -C₆)alkyl--O--C(O)--C-(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--(O)--, (C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl-O--, (C₁ -C₆)alkyl-C--(O), C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl-, di-(C₁ -C₆)alkylamino, --C(O)NH-(C₁ -C₆)-alkyl-, (C₁ -C₆)alkyl-C(O)--NH-(C₁ -C₆)alkyl, --NHC(O)H and --NHC(O)-(C₁ -C₆)alkyl; and wherein one of the phenyl moieties of said benzhydryl may optionally be replaced by naphthyl, thienyl, furyl or pyridyl;

R⁷ is hydrogen, phenyl or (C₁ -C₆)alkyl;

or R⁶ and R⁷, together with the carbon to which they are attached, form a saturated carbocyclic ring having from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur;

R⁸ and R⁹ are each independently selected from hydrogen, hydroxy, halo, amino, oxo (═O), nitrile, hydroxy-(C₁ -C₆)alkyl, (C₁ -C₆)alkoxy-(C₁ -C₆)alkyl, (C₁ -C₆)alkylamino, di-(C₁ -C₆)alkylamino, (C₁ -C₆)alkoxy, (C₁ -C₆)alkyl-O--C(O)--, (C₁ -C₆)alkyl-O--C(O)-(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--O, (C₁ -C₆)alkyl-C(O)(C₁ -C₆)alkyl-O--, (C₁ -C₆)alkyl-C(O)--, (C₁ -C₆)alkyl-C(O)(C₁ -C₆)alkyl-, and the radicals set forth in the definition of R⁶ ;

R¹⁰ is NHCR¹², NHCH₂ R¹², NHSO₂ R¹² or one of the radicals set forth in any of the definitions of R⁶, R⁸ and R⁹ ;

R¹¹ is oximino (═NOH) or one of the radicals set forth in any of the definitions of R⁶, R⁸ and R⁹ ; and

R¹² is (C₁ -C₆)alkyl, hydrogen, or phenyl(C₁ -C₆)alkyl or optionally substituted with (C₁ -C₆)alkyl; and

with the proviso that (a) when m is 0, R¹¹ is absent, (b) neither R⁸, R⁹, R¹⁰ nor R¹¹ can form, together with the carbon to which it is attached, a ring with R⁷, (c) when Q is a group of the formula VIII, R⁸ and R⁹ cannot be attached to the same carbon atom, (d) when R⁸ and R⁹ are attached to the same carbon atom, then either each of R⁸ and R⁹ is independently selected from hydrogen, fluoro, (C₁ -C₆)alkyl, hydroxy-(C₁ -C₆)alkyl and (C₁ -C₆)alkoxy-(C₁ -C₆)alkyl, or R⁸ and R⁹, together with the carbon to which they are attached, form a (C₃ -C₆) saturated carbocyclic ring that forms a spiro compound with the nitrogen-containing ring to which they are attached, (e) the nitrogen of formula (N) can not be double bonded to both Q and the substituted benzyl group to which it is attached, (f) when Q is a group of the formula VII and q is 2 and either R⁸ or R⁹ is 5-hydroxy-(C₁ -C₆)alkyl or 5-(C₁ -C₆)alkoxy-(C₁ -C₆)alkyl, then the other of R⁸ and R⁹ is either 5-(C₁ -C₆)alkyl or hydrogen; (g) when Q is a group of the formula VII and q is 2, then neither R⁸ nor R⁹ is 4-hydroxy-(C₁ -C₆)alkyl or 4-(C₁ -C₆)alkoxy-(C₁ -C₆)alkyl, and (h) when neither X¹, X² nor X³ is a fluorinated alkoxy group, at least one of R¹, R³, R⁴, R⁵, R⁶, R⁷ and R¹³ is an aryl group substituted with a fluorinated alkoxy group;

pharmaceutically acceptable acid addition and base salts of compounds of the formula N.

For example

(2S,3S)-2-phenyl-3-(2-trifluoromethoxybenzyl)]aminopiperidine--Compound 3; or a salt (e.g. hydrochloride) thereof; and

(2S,3S)-3-(2-methoxy-5-trifluoromethoxybenzyl )amino-2-phenylpiperidine--Compound 6.

WO 93/01159, i.e. compounds of the formula (O) or a salt or prodrug thereof ##STR20## wherein Q represents a group ##STR21## where W represents a bond, O, S, --CH₂ CH₂ --, --CH═CH-- or a group NR⁶, where R⁶ is H or C₁₋₆ alkyl and one or both of the phenyl rings may be replaced by a heteroaryl moiety;

X and Y each represent H or X and Y together form a group ═O;

Z represents O, S or NR⁸, where R⁸ represents H or C₁₋₆ alkyl;

R¹ and R² independently represent H; C₁₋₆ alkyl optionally substituted by hydroxy, cyano, COR^(a), COOR^(a), CONR^(a) R^(b), COC₁₋₄ alkylNR^(a) R^(b), CONR^(a) C₁₋₄ alkylCONR^(a) R^(b) or NR^(a) R^(b), (where R^(a) and R^(b) each independently represent H, C₁₋₆ alkyl, phenyl (optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl) or phenyl (C₁₋₄ alkyl) (optionally substituted in the phenyl ring by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl)); phenyl(C₁₋₄ alkyl), (optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl in the phenyl ring); C₂₋₆ alkylene; COC₁₋₆ alkylhalo; COR^(a) ; COOR^(a) ; CONHR^(a) ; COC₁₋₄ alkylNR^(a) R^(b) ; or CONR^(a) C₁₋₄ alkylCONR^(a) R^(b) ; (where R^(a) and R^(b) are as previously defined) or R¹ and R² together form a chain (CH₂)_(p) where p is 4 or 5 and where one non-terminal methylene group may optionally be replaced by an oxygen atom or a group NR^(x), where R^(x) is H or C₁₋₆ alkyl;

R³ represents H or C₁₋₆ alkyl;

R⁴ represents H, C₁₋₆ alkyl or phenyl (optionally substituted by one or more of C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, SR^(c), SOR^(c), SO₂ R^(c), OR^(c), NR^(c) R^(d), NR^(c) COR^(d), NR^(c) COOR^(d), COOR^(c) or CONR^(c) R^(d), where R^(c) and R^(d) each independently represent H, C₁₋₆ alkyl, phenyl or trifluoromethyl);

R⁵ represents (CH₂)_(q) phenyl, wherein q is 0, 1, 2 or 3 which may optionally be substituted in the phenyl ring by one or more of C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, SR^(c), SOR^(c), SO₂ R^(c), OR^(c), NR^(c) R^(d), NR^(c) COR^(d), NR^(c) COOR^(d), COOR^(c) or CONR^(c) R^(d), where R^(c) and R^(d) are as above defined;

each R⁷ and R⁸ independently represents C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, SR^(c), SOR^(c), SO₂ R^(c), OR^(c), NR^(c) R^(d), NR^(c) COR^(d), COOR^(c) or CONR^(c) R^(d) where R^(c) and R^(d) are as above defined; and

m and n independently represent 0, 1, 2, 3 or 4.

WO 93/01160, i.e. compounds of the formula (P) or a salt or prodrug thereof ##STR22## wherein Q represents R⁹ CR¹⁰ R¹¹ or CH₂ R⁹ CR¹⁰ R¹¹ where R⁹ is H or hydroxy and R¹⁰ and R¹¹ each independently represent optionally substituted phenyl, optionally substituted benzyl, C₅₋₇ cycloalkyl or (C₅₋₇ cycloalkyl)methyl;

R¹ and R² independently represent H; C₁₋₆ alkyl optionally substituted by hydroxy, cyano, COR^(a), COOR^(a), CONR^(a) R^(b), COC₁₋₆ alkylNR^(a) R^(b), CONR¹² C₁₋₆ alkylOR^(a), CONR¹² C₁₋₆ alkylCONR^(a) R^(b) or NR^(a) R^(b) (where R^(a) and R^(b) each independently represent H, C₁₋₆ alkyl, phenyl (optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl), phenyl (C₁₋₄ alkyl) (optionally substituted in the phenyl ring by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl) or R^(a) and R^(b) together form a chain (CH₂)_(p) optionally substituted by oxo where p is 4 or 5 and where one methylene group may optionally be replaced by an oxygen atom or a group NR^(x), where R^(x) is H or C₁₋₆ alkyl, and R¹² represents H, C₁₋₆ alkyl, phenyl (optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl) or phenyl (C₁₋₄ alkyl) (optionally substituted in the phenyl ring by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl); phenyl (C₁₋₄ alkyl) (optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl in the phenyl ring); C₂₋₆ alkenyl; C₂₋₆ alkynyl; COR^(a) ; COOR^(a) ; COC₁₋₆ alkylhalo; COC₁₋₆ alkylNR^(a) R^(b) ; CONR¹² C₁₋₆ alkylCONR^(a) R^(b) ; CONR^(a) R^(b) ; or SO₂ R^(a) ; (where R^(a), R^(b) and R¹² are as previously defined) or R¹ and R² together form chain (CH₂)_(q) optionally substituted by oxo where q is 4 or 5 and where one methylene group may optionally be replaced by an oxygen atom or a group NR^(x), where R^(x) is H or C₁₋₆ alkyl;

R³ represents H, C₁₋₆ alkyl or C₂₋₆ alkenyl;

R⁴ represents C₁₋₃ alkyl substituted by a phenyl group which may itself optionally be substituted by one or more of C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, SR^(c), SOR^(c), SO₂ R^(c), OR^(c), NR^(c) R^(d), NR^(c) COR^(d), NR^(c) COOR^(d), COOR^(c) and CONR^(c) R^(d), where R^(c) and R^(d) independently represent H, C₁₋₆ alkyl, phenyl or trifluoromethyl;

X and Y each represent H, or X and Y together represent a group ═O; and

Z represents O, S or NR⁷, where R⁷ represents H or C₁₋₆ alkyl;

with the exception of

DL-diphenylalanine benzyl ester;

2-benzamido-3,3-diphenylpropanoyl benzamide; and

2-benzamido-3,4-diphenyl-butanoyl benzamide.

WO 93/01165; i.e. compounds of the formula (Q) or a salt or prodrug thereof ##STR23## wherein Q represents optionally substituted phenyl, optionally substituted heteroaryl or optionally substituted naphthyl;

X and Y each represent H, C₁₋₆ alkyl, C₂₋₆ alkenyl or X and Y together form a group ═O;

Z represents O or S;

R¹ represents H; C₁₋₆ alkyl optionally substituted by hydroxy, cyano, COR^(a), COOR^(a), CONR^(a) R^(b), COC₁₋₄ alkylNR^(a) R^(b), CONR^(a) C₁₋₄ alkylCONR^(a) R^(b), (where R^(a) and R^(b) each independently represent H, C₁₋₆ alkyl, phenyl optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo or trifluoromethyl or phenyl (C₁₋₄ alkyl) optionally substituted in the phenyl ring by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo or trifluoromethyl); phenyl(C₁₋₄ alkyl), (optionally substituted in the phenyl ring by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo or trifluoromethyl); C₂₋₆ alkylene; COR^(a) ; COOR^(a) CONHR^(a) ; COC₁₋₆ alkylhalo; COC₁₋₆ alkylNR^(a) R^(b) ; or CONR^(a) C₁₋₆ alkylCONR^(a) R^(b), where R^(a) and R^(b) are as previously defined;

R² represents C₁₋₆ alkyl substituted by hydroxy, cyano, COR^(a), COO R^(a), CONR^(a) R^(b), COC₁₋₄ alkylNR^(a) R^(b), CONR^(a) C₁₋₄ alkylCONR^(a) R^(b) or NR^(a) R^(b), (where R^(a) and R^(b) are as above defined); phenyl(C₁₋₄ -alkyl), (optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl in the phenyl ring); C₂₋₆ alkylene; COR^(a) ; COOR^(a) ; CONHR^(a) ; COC₁₋₆ alkylhalo; COC₁₋₆ alkylNR^(a) R^(b) ; or CONR^(a) C₁₋₆ alkylCONR^(a) R^(b), where R^(a) and R^(b) are as previously defined;

or R¹ and R² together form a chain (CH₂)_(p) optionally substituted by oxo; where p is 4 or 5 and where one methylene group may optionally be replaced by an oxygen atom or a group NR^(x), where R^(x) is H or C₁₋₆ alkyl;

R³ represents H or C₁₋₆ alkyl;

R⁴ represents H, C₁₋₆ alkyl or phenyl (optionally substituted by one or more of C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, SR^(c), SOR^(c), SO₂ R^(c), OR^(c), NR^(c) R^(d), NR^(c) COR^(d), NR^(c) COOR^(d), COOR^(c) or CONR^(c) R^(d), where R^(c) and R^(d) each independently represent H, C₁₋₆ alkyl, phenyl or trifluoromethyl); and

R⁵ represents (CH₂)_(q) phenyl, wherein q is 0, 1, 2 or 3, which may optionally be substituted in the phenyl ring by one or more of C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, SR^(c), SOR^(c), SO₂ R^(c), OR^(c), NR^(c) R^(d), NR^(c) COR^(d), NR^(c) COOR^(d), COOR^(c) or CONR^(c) R^(d), where R^(c) and R^(d) are as above defined.

WO 93/01169, i.e. compounds of the formula (R) or a salt or prodrug thereof ##STR24## wherein q represents optionally substituted phenyl, optionally substituted naphthyl, optionally substituted indolyl, optionally substituted benzthiophenyl, optionally substituted benzofuranyl, optionally substituted benzyl or optionally substituted indazolyl;

z represents O, S or NR⁸, where R⁸ is H or C₁₋₆ alkyl;

X and Y each represent H or X and Y together form a group ═O;

R¹ and R² each independently represent H; C₁₋₆ alkyl, optionally substituted by hydroxy, cyano, COR^(c), CO₂ R^(c), CONR^(c) R^(d), or NR^(c) R^(d) (where R^(c) and R^(d) each independently represent H, C₁₋₁₂ alkyl or phenyl optionally substituted by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo or trifluoromethyl); phenyl(C₁₋₄ alkyl) (optionally substituted in the phenyl ring by one or more of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl); COR^(c) ; CO₂ R^(c) ; CONR^(c) R^(d) ; CONR^(c) COOR^(d) ; or SO₂ R^(c), where R^(c) and R^(d) are as above defined;

R³ represents H or C₁₋₆ alkyl; and

R⁴ represents H, C₁₋₆ alkyl or phenyl (optionally substituted by 1, 2 or 3 groups selected from C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, cyano, nitro trifluoromethyl, trimethylsilyl, OR^(a), SR^(a), SOR^(a), NR^(a) R^(b), NR^(a) COR^(b), NR^(a) CO₂ R^(b) ; CO₂ R^(a) or CONR^(a) R^(b), where R^(a) and R^(b) independently represent H, C₁₋₆ alkyl, phenyl or trifluoromethyl); and

R⁵ represents phenyl (optionally substituted by 1, 2 or 3 groups selected from C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, OR^(a), SR^(a), SOR^(a), NR^(a) R^(b), NR^(a) COR^(b), NR^(a) CO₂ R^(b), CO₂ R^(a) or CONR^(a) R^(b), where R^(a) and R^(b) independently represent H, C₁₋₆ alkyl, phenyl or trifluoromethyl); with the exception of

benzyl 3-(3-indolyl)-2-amino propionate;

4-nitrobenzyl 3-(3-indolyl)-2-aminopropionate;

4-nitrobenzyl 2-(1,1-dimethylethoxycarbonylamino)-3-(3-indolyl)propionate;

benzyl 2-(1,1-dimethylethoxycarbonylamino)-3-(3-indolyl)propionate;

4-methoxybenzyl 2-(1,1-dimethylethoxycarbonylamino)-3-(3-indolyl)propionate;

2,4,6-trimethylbenzyl 3-(3-indolyl)-2-aminopropionate; benzyl 3-(3-indolyl)-2-((4-methylphylsulphonamido)propionate;

benzyl 2-(1,1-dimethylpropyloxycarbonylamino)-3-(3-indolyl)propionate;

4-nitrobenzyl 2-acetamido-3-(3-indolyl)propionate; benzyl 3-(1-naphthyl)-2-aminopropionate;

benzyl 3-(1-naphthyl)-2-(1,1-dimethylethoxycarbonyl amino)propionate;

benzyl 3-(2-naphthyl)-2-aminopropionate;

N-methyl-N-benzyl 3-(2-naphthyl)-2-(1,1-dimethylethoxycarbonylamino)propionamide;

N-methyl-N-(4-fluorobenzyl)-3-(2-naphthyl)-2-(1,1-dimethylethoxycarbonylamino)propionamide;

N-methyl-N-(2-fluorobenzyl)-3-(2-naphthyl)-2-(1,1-dimethylethoxycarbonylamino)propionamide;

N-methyl-N-benzyl-3-(1-naphthyl)-2-(1,1-dimethylethoxycarbonylamino)propionamide;

N-methyl-N-(4-fluorobenzyl)-3-(2-naphthyl)-2-aminopropionamide;

N-methyl-N-(3-fluorobenzyl)-3-(2-naphthyl)-2-aminopropionamide;

N-methyl-N-(3-fluorobenzyl)-3-(2-naphthyl)-2-aminopropionamide,

N-methyl-N-benzyl-3-(2-naphthyl)-2-aminopropionamide;

N-methyl-N-(3-fluorobenzyl)-3-(2-naphthyl)-2-(1,1-dimethylethoxycarbonylamino)propionamide;

benzyl 3-phenyl-2-aminopropionate; and

4-nitrobenzyl 3-phenyl-2-aminopropionate.

WO 93/01170; i.e. compounds of the formula (S) ##STR25## wherein Y is (CH₂)_(n) wherein n is an integer from 1 to 6, and wherein any one of the carbon-carbon single bonds in said (CH₂)_(n) may optionally be replaced by a carbon-carbon double bond, and wherein any one of the carbon atoms of said (CH₂)_(n) may optionally be substituted with R⁴, and wherein any one of the carbon atoms of said (CH₂)_(n) may optionally be substituted with R⁷ ;

m is an integer from 0 to 8, and any one of the carbon-carbon single bonds of (CH₂)_(m) may optionally be replaced by a carbon-carbon double bond or a carbon-carbon triple bond, and any one of the carbon atoms of said (CH₂)_(m) may be optionally substituted with R⁸,

R¹ is hydrogen or (C₁ -C₈)alkyl optionally substituted with hydroxy, alkoxy or fluoro;

R² is a radical selected from hydrogen, (C₁ -C₆) straight or branched alkyl, (C₃ -C₇)cycloalkyl wherein one of the carbon atoms may optionally be replaced by nitrogen, oxygen or sulfur, aryl selected from phenyl and naphthyl; heteroaryl selected from indanyl, thienyl, furyl, pyridyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, triazolyl, tetrazolyl and quinolyl; phenyl (C₂ -C₆)alkyl, benzhydryl and benzyl, wherein each of said awl and heteroaryl groups and the phenyl moieties of said benzyl, phenyl (C₂ -C₆)alkyl and benzhydryl may optionally be substituted with one or more substituents independently selected from halo, nitro, (C₁ -C₆)alkyl, (C₁ -C₆)alkoxy, trifluoromethyl, amino, (C₁ -C₆)alkylamino, (C₁ -C₆)alkyl-O--C(O)--, (C₁ -C₆)alkyl-O--C(O)--, (C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--O--, (C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl-O--, (C₁ -C₆)alkyl-C(O)--, (C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl-, di-(C₁ -C₆)alkylamino, --C(O)NH(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--NH-(C₁ -C₆)alkyl, --NH(O)CH and --NH(O)C₁ -C₆)alkyl; and wherein one of the phenyl moieties of said benzhydryl may optionally be replaced by naphthyl, thienyl, furyl or pyridyl;

R⁵ is hydrogen, phenyl or (C₁ -C₆)alkyl;

or R² and R⁵, together with the carbon to which they are attached, form a saturated carbocyclic ring having from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur;

R³ is aryl selected from phenyl and naphthyl; heteroaryl selected from indanyl, thienyl, furyl, pyridyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, triazolyl, tetrazolyl and quinolyl; and cycloalkyl having 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by nitrogen, oxygen or sulfur; wherein each of said aryl and heteroaryl groups may optionally be substituted with one or more substituents, and said (C₃ -C₇)cycloalkyl may optionally be substituted with one or two substituents, each of said substituents being independently selected from halo, nitro, (C₁ -C₆)alkyl, (C₁ -C₆)alkoxy, trifluoromethyl, phenyl, amino, (C₁ -C₆)alkylamino, --C(O)--NH-(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--NH-(C₁ -C₆)alkyl, --NHC(O)H and --NHC(O)-(C₁ -C₆)alkyl; and

R⁴ and R⁷ are each independently selected from hydrogen, hydroxy, halo, amino, oxo (═O), nitrile, (C₁ -C₆)alkylamino, di-(C₁ -C₆)alkylamino, (C₁ -C₆)alkoxy, (C₁ -C₆)alkyl-O--C(O)--, (C₁ -C₆)alkyl-O--C(O)-(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--O--, (C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl-O--, hydroxy-(C₁ -C₆)alkyl, (C₁ -C₆)alkoxy(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--, (C₁ -C₆)alkyl-C(O)-C₁ -C₆)alkyl- and the radicals set forth in the definition of R²,

R⁶ is NHC(O)R⁹, NHCH₂ R⁹, SO₂ R⁹ or one of the radicals set forth in any of the definitions of R², R⁴ and R⁷ ;

R⁸ is oximino (═NOH) or one of the radicals set forth in any of the definitions of R², R⁴ and R⁷ ;

R⁹ is (C₁ -C₆)alkyl, hydrogen, phenyl or phenyl (C₁ -C₆)alkyl;

with the proviso that (a) when m is 0, R⁸ is absent, (b) neither R⁴, R⁶, R⁷ nor R⁸ can form, together with the carbon to which it is attached, a ring with R⁵, (c) when R⁴ and R⁷ are attached to the same carbon atom, then either each of R⁴, and R⁷ is independently selected from hydrogen, fluoro and (C₁ -C₆)alkyl, or R⁴ and R⁷, together with the carbon to which they are attached, form a (C₃ -C₆) saturated carbocyclic ring that forms a spiro compound with the nitrogen-containing ring to which they are attached, (d) when n is 2 and either R⁴ or R⁷ is 5-hydroxy(C₁ -C₆)alkyl or 5-(C₁ -C₆)alkoxy-(C₁ -C₆)alkyl, then the other of R⁴ and R⁷ is hydrogen, (e) when n is 2, neither R⁴ nor R⁷ is 4-hydroxy(C₁₋₆)alkyl or 4-(C₁ -C₆)alkoxy (C₁ -C₆)alkyl, and (f) in all compounds of the formula (S), either R³ is aryl substituted with at least one phenyl group, or one or both of R⁴ and R⁷ is hydroxy-(C₁ -C₆)alkyl or (C₁ -C₆)alkoxy(C₁ -C₆)alkyl.

For example

(2S,3S)-3-(5-carbomethoxy-2-methoxybenzyl)amino-2-phenylpiperidine hydrochloride--Compound 4;

Preferred tachykinin antagonists for use in the present invention include those compounds generically and specifically disclosed in EP 522808, WO 92/17449, WO 93/00331, WO 93/01170 and EP528495.

The tachykinin antagonists may be administered as the raw chemical but the active ingredients are preferably presented as a pharmaceutical formulation. Suitable pharmaceutical formulations are described in the above referenced patent specifications.

Thus, the tachykinin antagonists may be formulated for oral, buccal, parenteral, depot or rectal administration or in a form suitable for administration by inhalation or insufflation (either through the mouth or nose). Oral and parenteral formulations are preferred.

For oral administration, the pharmaceutical compositions may take the form of, for example, tablets or capsules prepared by conventional means with pharmaceutically acceptable excipients such as binding agents (e.g. pregelatinised maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose); fillers (e.g. lactose, microcrystalline cellulose or calcium hydrogen phosphate); lubricants (e.g. magnesium stearate, talc or silica); disintegrants (e.g. potato starch or sodium starch glycollate); or wetting agents (e.g. sodium lauryl sulphate). The tablets may be coated by methods well known in the art. Liquid preparations for oral administration may take the form of, for example, solutions, syrups or suspensions, or they may be presented as a dry product for constitution with water or other suitable vehicle before use. Such liquid preparations may be prepared by conventional means with pharmaceutically acceptable additives such as suspending agents (e.g. sorbitol syrup, cellulose derivatives or hydrogenated edible fats); emulsifying agents (e.g. lecithin or acacia); non-aqueous vehicles (e.g. almond oil, oily esters, ethyl alcohol or fractionated vegetable oils); and preservatives (e.g. methyl or propyl-p-hydroxybenzoates or sorbic acid). The preparations may also contain buffer salts, flavouring, colouring and sweetening agents as appropriate.

Preparations for oral administration may be suitably formulated to give controlled release of the active compound.

For buccal administration the composition may take the form of tablets or lozenges formulated in conventional manner.

The tachykinin antagonists may be formulated for parenteral administration by bolus injection or continuous infusion. Formulations for injection may be presented in unit dosage form e.g. in ampoules or in multi-dose containers, with an added preservative. The compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising and/or dispersing agents. Alternatively, the active ingredient may be in powder form for constitution with a suitable vehicle, e.g. sterile pyrogen-free water, before use.

The tachykinin antagonists may also be formulated in rectal compositions such as suppositories or retention enemas, e.g. containing conventional suppository bases such as cocoa butter or other glycerides.

The tachykinin antagonists may also be formulated as depot preparations. Such long acting formulations may be administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection. Thus, for example, the compounds of the invention may be formulated with suitable polymeric or hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt.

For intranasal administration, the tachykinin antagonists may be formulated as solutions for administration via a suitable metered or unit dose device or alternatively as a powder mix with a suitable carrier for administration using a suitable delivery device.

Suitable dose ranges are also described in the above referenced patent specifications, that is to say that for use as anti-emetics the compounds may be used at doses appropriate for other conditions for which tachykinin antagonists are known to be useful. It will be appreciated that it may be necessary to make routine variations to the dosage, depending on the age and condition of the patient, and the precise dosage will be ultimately at the discretion of the attendant physician or veterinarian. The dosage will also depend on the route of administration and the particular compound selected. A suitable dose range is for example 0.1 mg/kg to about 400mg/kg bodyweight per day.

The tachykinin antagonists may, if desired, be administered in combination with one or more other therapeutic agents and formulated for administration by any convenient route in a conventional manner. Appropriate doses will be readily appreciated by those skilled in the art. For example, the tachykinin antagonists may be administered in combination with a systemic anti-inflammatory corticosteroid such as methyl prednisolone or dexamethasone, or a 5HT₃ antagonist such as ondansetron, granisetron or metoclopramide.

Biological Data

The anti-emetic activity of the test compounds 1, 2 (as hydrochloride salt), 3, 4 and 5 (as racemates) and 6 (as single enantiomer) defined hereinbefore was demonstrated by their ability to inhibit cisplatin- or radiation-induced emesis in the ferret.

Cisplatin Test

In this model of emesis the onset of retching and vomiting occurs approximately 1 hour after the administration of cisplatin (200 mg/m² i.p.). At first retch in response to cisplatin, the test compound was administered (e.g. i.p., p.o., i.v., s.c., i.c.v.) and its effect on emesis determined by comparison with appropriate controls (e.g. water).

Radiation Test

In this model of emesis the onset of retching and vomiting occurs approximately 20 minutes after whole body irradiation (2 Grey.tbd.200 Rads). The test compound is administered (e.g. i.p., p.o., i.v., s.c.) immediately after irradiation and its effect on emesis determined by comparison with appropriate controls. In the case of compound 6, this test compound was administered 90 minutes before whole body irradiation.

Test compounds 1 to 6 inhibited emesis in the above tests at the doses shown:

    ______________________________________                                         Compound       Dose mg/kg Test                                                 ______________________________________                                         1              10     (i.p.)  cisplatin                                        2              1.0    (s.c.)  radiation                                        3              10     (s.c.)  cisplatin                                        4              10     (s.c.)  cisplatin                                        5              10     (s.c)   cisplatin                                        6              0.03   (s.c)   radiation                                        ______________________________________                                    

Reference Example

The compound (2S,3S)-3-(2-methoxybenzylamino)-2-phenyl piperidine inhibited cisplatin-induced emesis in the ferret when administered at a dose of 3 mg/kg i.p. The (2R,3R) enantiomer of the above compound, which is 1000-fold less active as an NK₁ receptor antagonist than the (2S,3S) enantiomer, was inactive in the cisplatin emesis test at the same dose. 

We claim:
 1. A method for the treatment or prophylaxis of emesis of a mammal, comprising administering to said mammal an effective amount of an NK₁ receptor antagonist of formula J, N, S or G: ##STR26## wherein R¹ is aryl selected from the group consisting of indanyl, phenyl and naphthyl; heteroaryl selected from the group consisting of thienyl, furyl, pyridyl and quinolyl; or cycloalkyl having 3 to 7 carbon atoms, wherein one of said carbon atoms may optionally be replaced by nitrogen, oxygen or sulfur; wherein each of said aryl and heteroaryl groups may optionally be substituted with one or more substituents, and said (C₃ -C₇)cycloalkyl may optionally be substituted with one or two substituents, said substituents being independently selected from the group consisting of chloro, fluoro, bromo, iodo, nitro, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluoro groups, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluoro groups, amino, (C₁ -C₁₀)alkyl-S--, (C₁ -C₁₀)alkyl-S(O)--, (C₁ -C₁₀)alkyl-SO₂ --, phenyl, phenoxy, (C₁ -C₁₀)alkyl-SO₂ NH--, (C₁ -C₁₀)alkyl-SO₂ NH-(C₁ -C₁₀)alkyl-, (C₁ -C₁₀)alkylamino-di(C₁ -C₁₀)alkyl-, cyano, hydroxy, cycloalkoxy having 3 to 7 carbon atoms, (C₁ -C₆)alkylamino, (C₁ -C₆)dialkylamino, HC(O)NH-- and (C₁ -C₁₀)alkyl-C(O)--NH--, wherein the nitrogen atoms of said amino and (C₁ -C₆)alkylamino groups may optionally be protected with an appropriate protecting group; andR² is thienyl, benzhydryl, naphthyl or phenyl optionally substituted with from one to three substituents independently selected from the group consisting of chloro, bromo, fluoro, iodo, cycloalkoxy having 3 to 7 carbon atoms, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluoro groups, and (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluoro groups; ##STR27## wherein X¹ is hydrogen, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms or (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms; X² and X³ are independently selected from the group consisting of hydrogen, halo, nitro, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms, (C₁ -C₁₀)alkoxy optionally substituted with form one to three fluorine atoms, trifluoromethyl, hydroxy, phenyl, cyano, amino, (C₁ -C₆)-alkylamino, di-(C₁ -C₆)alkylamino, --C(O)--NH-(C₁ -C₆)-alkyl, (C₁ -C₆)alkyl-C(O)--NH-(C₁ -C₆)alkyl, hydroxy, (C₁ -C₄)alkyl, (C₁ -C₄)alkyoxy(C₁ -C₄)alkyl, --NHC(O)H and --NHC(O)-(C₁ -C₆)alkyl; and Q is a group of the formula ##STR28## wherein R¹ is a radical selected from the group consisting of furyl, thienyl, pyridyl, indolyl, biphenyl and phenyl optionally substituted with one or two substituents independently selected from the group consisting of halo, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms, carboxy, benzyloxycarbonyl and (C₁ -C₃)alkoxy-carbonyl; R¹³ is selected from the group consisting of (C₃ -C₄ ₄) branched alkyl, (C₅ -C₆) branched alkenyl, (C₅ -C₇)cycloalkyl, and the radicals named in the definition of R¹ ; R² is hydrogen or (C₁ -C₆)alkyl; R³ is phenyl, biphenyl, naphthyl, pyridyl, benzhydryl, thienyl or furyl, and R³ may optionally be substituted with from one to three substituents independently selected from the group consisting of halo, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms and (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms; Y is (CH₂)_(l) wherein l is an integer from one to three or Y is a group of the formula ##STR29## Z is oxygen, sulfur, amino, (C₁ -C₃)alkylamino or (CH₂)_(n) wherein n is zero, one or two; o is two or three; p is zero or one; R⁴ is furyl, thienyl, pyridyl, indolyl, biphenyl, or phenyl optionally substituted with one or two substituents independently selected from the group consisting of halo, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms, carboxy, (C₁ -C₃)alkoxycarbonyl and benzyloxycarbonyl; R⁵ is thienyl, biphenyl or phenyl optionally substituted with one or two substituents independently selected from the group consisting of halo, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms and (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms; each of the two dashed lines in formula (N) and the dashed line in formula (II) represents an optional double bond that may optionally exist when Q is a group of the formula (II); X is (CH₂)_(q) wherein q is an integer from 1 to 6, and wherein any one of the carbon-carbon single bonds in said (CH₂)_(q) may optionally be replaced by a carbon-carbon double bond, and wherein any one of the carbon atoms of said (CH₂)_(q) may optionally be substituted with R⁸, and wherein any one of the carbon atoms of said (CH₂)_(q) may be substituted with R⁹ ; m is an integer from 0 to 8, and any one of the carbon-carbon single bonds of (CH₂)_(m) may optionally be replaced by a carbon-carbon double bond, or a carbon-carbon triple bond, and any one of the carbon atoms of said (CH₂)_(m) may optionally be substituted with R¹¹ ; R⁶ is a radical selected from the group consisting of hydrogen, (C₁ -C₆) straight or branched alkyl, (C₃ -C₇)cycloalkyl wherein one of the carbon atoms may optionally be replaced by nitrogen, oxygen or sulfur; aryl selected from the group consisting of biphenyl, phenyl, indanyl and naphthyl; heteroaryl selected from the group consisting of thienyl, furyl, pyridyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, triazolyl, tetrazolyl and quinolyl; phenyl(C₂ -C₆)alkyl, benzhydryl and benzyl, wherein each of said aryl and heteroaryl groups and the phenyl moieties of said benzyl, phenyl(C₂ -C₆)alkyl and benzhydryl may optionally be substituted with one or more substituents independently selected from the group consisting of halo, nitro, (C₁ -C₁₀)alkyl optionally substituted with from one to three fluorine atoms, (C₁ -C₁₀)alkoxy optionally substituted with from one to three fluorine atoms, amino, hydroxy-(C₁ -C₆)alkyl, (C₁ -C₆)alkoxy-(C₁ -C₆)alkyl, (C₁ -C₆)alkylamino, (C₁ -C₆)alkyl-O--C(O)--, (C₁ -C₆)alkyl-O--C(O)--C-(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C--(O)--(O)--, (C₁ -C₆)alkyl-C(O)(C₁ -C₆)alkyl-O--, (C₁ -C₆)alkyl-C(O), (C₁ -C₆)alkyl-C(O)(C₁ -C₆)alkyl-, di-(C₁ -C₆)alkylamino, --C(O)NH-(C₁ -C₆)-alkyl-, (C₁ -C₆)alkyl-C(O)--NH-(C₁ -C₆)alkyl, --NHC(O)H and NHC(O)-(C₁ -C₆)alkyl; and wherein one of the phenyl moieties of said benzhydryl may optionally be replaced by naphthyl, thienyl, furyl or pyridyl; R⁷ is hydrogen, phenyl or (C₁ -C₆)alkyl; or R⁶ and R⁷, together with the carbon to which they are attached, form a saturated carbocyclic ring having from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur; R⁸ and R⁹ are each independently selected from the group consisting of hydrogen, hydroxy, halo, amino, oxo (═O), nitrile, hydroxy-(C₁ -C₆)alkyl, (C₁ -C₆)-alkoxy-(C₁ -C₆)alkyl, (C₁ -C₆)alkylamino, di-(C₁ -C₆)alkylamino, (C₁ -C₆)alkoxy, (C₁ -C₆)alkyl-O--C(O)--, (C₁ -C₆)-alkyl-O--C(O)-(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--O, (C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl-O--, (C₁ -C₆)alkyl-C(O)--, (C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl-, and the radicals set forth in the definition of R⁶ ; R¹⁰ is NHCR¹², NHCH₂ R¹², NHSO₂ R¹², or one of the radicals set forth in any of the definitions of R⁶, R⁸ and R⁹ ; R¹¹ is oximino (═NOH) or one of the radicals set forth in any of the definitions of R⁶, R⁸ and R⁹ ; and R¹² is (C₁ -C₆)alkyl, hydrogen, phenyl(C₁ -C₆)alkyl or phenyl optionally substituted with (C₁ -C₆)alkyl, andwith the provisos that (a) when m is O, R¹¹ is absent; (b) neither R⁸, R⁹, R¹⁰ nor R¹¹ can form, together with the carbon to which it is attached, a ring with R⁷ ; (c) when Q is a group of the formula (VIII), R⁸ and R⁹ cannot be attached to the same carbon atom; (d) when R⁸ and R⁹ are attached to the same carbon atom, then either each of R⁸ and R⁹ is independently selected from hydrogen, fluoro, (C₁ -C₆)alkyl, hydroxy-(C₁ -C₆)alkyl and (C₁ -C₆)alkoxy-(C₁ -C₆)alkyl, or R⁸ and R⁹, together with the carbon to which they are attached, form a (C₃ -C₄ ₆) saturated carbocyclic ring that forms a spiro compound with the nitrogen-containing ring to which they are attached; (e) the nitrogen of formula (N) cannot be double bonded to both Q and the substituted benzyl group to which it is attached; (f) when Q is a group of the formula (VII) and q is 2 and either R⁸ or R⁹ is 5-hydroxy-(C₁ -C₆)alkyl or 5-(C₁ C₆)alkoxy-(C₁ -C₆)alkyl, then the other of R⁸ or R⁹ is either 5-(C₁ -C₆)alkyl or hydrogen; (g) when Q is a group of the formula (VII) and q is 2, then neither R⁸ nor R⁹ is 4-hydroxy-(C₁ -C₆)alkyl or 4-(C₁ -C₆)alkoxy-(C₁ -C₆)alkyl; and (h) when neither X¹, X² nor X³ is a fluorinated alkoxy group, at least one of R¹, R³, R⁴, R⁵, R⁶, R⁷ and R¹³ is an aryl group substituted with a fluorinated alkoxy group;and pharmaceutically acceptable acid addition and base salts of compounds of the formula (N); ##STR30## wherein Y is (CH₂)_(n) wherein n is an integer from 1 to 6, and wherein any one of the carbon-carbon single bonds in said (CH₂)_(n) may optionally be replaced by a carbon-carbon double bond, and wherein any one of the carbon atoms of said (CH₂)_(n) may optionally be substituted with R⁴, and wherein any one of the carbon atoms of said (CH₂)_(n) may be substituted with R⁷ ; m is an integer from 0 to 8, and any one of the carbon-carbon single bonds of (CH₂)_(m) may optionally be replaced by a carbon-carbon double bond, or a carbon-carbon triple bond, and any one of the carbon atoms of said (CH₂)_(m) may be optionally substituted with R⁸ ; R¹ is hydrogen or (C₁ -C₈)alkyl optionally substituted with hydroxy, alkoxy or fluoro; R² is a radical selected from the group consisting of hydrogen, (C₁ -C₆) straight or branched alkyl, (C₃ -C₄ ₇)cycloalkyl wherein one of the carbon atoms may optionally be replaced by nitrogen, oxygen or sulfur; aryl selected from the group consisting of phenyl and naphthyl; heteroaryl selected from the group consisting of indanyl, thienyl, furyl, pyridyl, thiazolyl, isothiazolyl, oxazolyl, triazolyl, tetrazolyl and quinolyl; phenyl(C₂ -C₆)alkyl, benzhydryl and benzyl, wherein each of said aryl and heteroaryl groups and the phenyl moieties of said benzyl, phenyl(C₂ -C₆)alkyl and benzhydryl may optionally be substituted with one or more substituents independently selected from halo, nitro, (C₁ -C₆)alkyl, (C₁ -C₆)alkoxy, trifluoromethyl, amino, (C₁ -C₆)alkylamino, (C₁ -C₆)alkyl-O--C--(O)--, (C₁ -C₆)alkyl-O--C(O)-(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--O, (C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl-O--, (C₁ -C₆)alkyl-C(O)--, (C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl-, di-(C₁ -C₆)alkyl-amino, --C(O)NH-(C₁ -C₆)alkyl-, (C₁ -C₆)alkyl-C(O)--NH-(C₁ -C₆)alkyl, --NH(O)CH and --NH(O)C-(C₁ -C₆)alkyl; and wherein one of the phenyl moieties of said benzhydryl may optionally be replaced by naphthyl, thienyl, furyl or pyridyl; R⁵ is hydrogen, phenyl or (C₁ -C₆)alkyl; or R² and R⁵, together with the carbon to which they are attached, form a saturated carbocyclic ring having from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur; R³ is aryl selected from the group consisting of phenyl and naphthyl; heteroaryl selected from the group consisting of indanyl, thienyl, furyl, pyridyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, triazolyl, tetrazolyl and quinolyl; and cycloalkyl having 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by nitrogen, oxygen or sulfur; wherein each of said aryl and heteroaryl groups may optionally be substituted with one or more substituents, and said (C₃ -C₇)cycloalkyl may optionally be substituted with one or two substituents, each of said substituents being independently selected from the group consisting of halo, nitro, (C₁ -C₆)alkyl, (C₁ -C₆)alkoxy, trifluoromethyl, phenyl, amino, (C₁ -C₆)alkylamino, --C(O)NH-(C₁ -C₆)alkyl, (C₁ -C₆)alkyl C(O)--NH-(C₁ -C₆)alkyl, --NHC(O)H and --NHC(O)-(C₁ -C₆)alkyl; R⁴ and R⁷ are each independently selected from the group consisting of hydrogen, hydroxy, halo, amino, oxo (═O), nitrile, (C₁ -C₆)alkylamino, di-(C₁ -C₆)alkylamino, (C₁ -C₆)alkoxy, (C₁ -C₆)alkyl-O--C(O)--, (C₁ -C₆)alkyl-O--C(O)-(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--O, (C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl-O, hydroxy-(C₁ -C₆)alkyl, (C₁ -C₆)alkoxy(C₁ -C₆)alkyl, (C₁ -C₆)alkyl-C(O)--, (C₁ -C₆)alkyl-C(O)-(C₁ -C₆)alkyl- and the radicals set forth in the definition of R² ; R⁶ is NHC(O)R⁹, NHCH₂ R⁹, SO₂ R⁹, or one of the radicals set forth in any of the definitions of R², R⁴ and R⁷ ; R⁸ is oximino (═NOH) or one of the radicals set forth in any of the definitions of R², R⁴ and R⁷ ; R⁹ is (C₁ -C₆)alkyl, hydrogen, phenyl or phenyl(C₁ -C₆)alkyl;with the provisos that (a) when m is O, R⁸ is absent; (b) neither R⁴, R⁶, R⁷ nor R⁸ can form, together with the carbon to which it is attached, a ring with R⁵ ; (c) when R⁴ and R⁷ are attached to the same carbon atom, then either each of R⁴ and R⁷ is independently hydrogen, fluoro or (C₁ -C₆)alkyl, or R¹ and R⁷, together with the carbon to which they are attached, form a (C₃ -C₆) saturated carbocyclic ring that forms a spiro compound with the nitrogen-containing ring to which they are attached; (d) when n is 2 and either R⁴ or R⁷ is 5-hydroxy(C₁ -C₆)alkyl or 5-(C₁ -C₆)alkoxy-(C₁ -C₆)alkyl, then the other of R⁴ and R⁷ is hydrogen; (e) when n is 2, neither R⁴ nor R⁷ is 4-hydroxy(C₁ -C₆)alkyl or 4-(C₁ -C₆)alkoxy(C₁ -C₆)alkyl; and (f) in all compounds of the formula (S), either R³ is aryl substituted with at least one phenyl group, or one or both of R⁴ and R⁷ is hydroxy-(C₁ -C₆)alkyl or (C₁ --C₆)alkoxy(C₁ -C₆)alkyl; ##STR31## wherein n is 1, 2 or 3 and where any carbon atom of (CH₂)_(n) may be substituted by R⁴ and/or R⁵ ; X represents O or S; R¹ represents phenyl optionally substituted by 1, 2 or 3 groups selected from the group consisting of C₁₋₆ alkyl, C₂₋₆ alkenyl; C₂₋₆ alkynyl, halo, cyano, nitro, trifluoromethyl, trimethylsilyl, ---OR^(a), SR^(a), SOR^(a), SO₂ R^(a), --NR^(a) R^(b), --NR^(a) COR^(b), --NR^(a) CO₂ R^(b), CO₂ R^(a), or --CONR^(a) R^(b) ; R² represents aryl selected from the group consisting of phenyl and naphthyl; heteroaryl selected from the group consisting of indazolyl, thienyl, furyl, pyridyl, thiazolyl, tetrazolyl and quinolyl; benzhydryl; or benzyl; wherein each aryl or heteroaryl moiety may be substituted by C₁₋₆ alkyl, C₁₋₆ alkoxy, halo or trifluoromethyl; R⁴ and R⁵ each independently represent H, halo, CH₂ OR⁹, C₁₋₆ alkyl, oxo, CO₂ R¹⁰ or CONR¹⁰ R¹¹ ; R⁸ represents H, COR⁹, CO₂ R¹⁰, COCONR¹⁰ R¹¹, COCO₂ R¹⁰ or C₁₋₆ alkyl optionally substituted by a group selected from the group consisting of CO₂ R¹⁰, CONR¹⁰ R¹¹, hydroxy, cyano, COR⁹, NR¹⁰ R¹¹, C(NOH)NR¹⁰ R¹¹, CONHphenyl-(C₁₋₄ alkyl), COCO₂ R¹⁰, COCONR¹⁰ R¹¹ and phenyl optionally substituted by one or more substituents selected from the group consisting of C₁₋₆ alkyl, C₁₋₆ alkoxy, halo and trifluoromethyl; R^(a) and R^(b) each independently represent H, C₁₋₆ alkyl, phenyl or trifluoromethyl; R⁹ represents H, C₁₋₆ alkyl or phenyl; and R¹⁰ and R¹¹ each independently represent H or C₁₋₆ alkyl.
 2. A method according to claim 1 wherein said emesis is induced by cancer chemotherapeutic agents, radiation sickness, radiation therapy, poisons, toxins, pregnancy, vestibular disorders, post-operative sickness, gastrointestinal obstruction, reduced gastrointestinal motility, visceral pain, migraine, increased intercranial pressure, decreased intercranial pressure, or opioid analgesics.
 3. A method according to claim 2 wherein said emesis is induced by a cancer chemotherapeutic agent, radiation sickness or radiation therapy.
 4. A method as claimed in claim 3 wherein the NK₁ receptor antagonist is administered to said mammal prior to administration of a cancer chemotherapeutic agent.
 5. A method as claimed in claim 4 wherein the cancer chemotherapeutic agent is selected from the group consisting of cyclophosphamide, carmustine, lomustine, chloroambucil, dactinomycin, doxorubicin, mitomycin-C, bleomycin, cytarabine, methotrexate, 5-fluoroacil, etoposide, vinblastine, vincristine, cisplatin, decarbazine, procarbazine, hydroxyurea, and combinations thereof.
 6. A method as claimed in claim 5 wherein the cancer chemotherapeutic agent is cisplatin.
 7. A method as claimed n claim 5 wherein the cancer chemotherapeutic agent is cyclophosphamide.
 8. A method as claimed in claim 3 wherein the NK₁ receptor antagonist is administered to the mammal prior to radiation therapy.
 9. A method according to claim 3 wherein said cancer chemotherapeutic agent is selected from the group consisting of from cyclophosphamide, carmustine, lomustine, chloroambucil, dactinomycin, doxoruibicin, mitomycin-C, bleomycin, cytarabine, methotrexate, 5-fluorouracil, etoposide, vinblastine, vincristine, cisplatin, decarbazine, procarbazine, hydroxyurea, and combinations thereof.
 10. A method according to claim 9 wherein said emesis is induced by cisplatin.
 11. A method according to claim 9 wherein said emesis is induced by cyclophosphamide.
 12. A method according to claim 1 wherein the tachykinin antagonist is a compound selected from:2-ammonium-1-((3,5-bis(trifluoromethyl)phenyl)methyloxy)-3,3-diphenylpropane; (2S,3S)-3-(2-methoxy-5-methylmercaptobenzylamino)-2-phenylpiperidine; (2S,3S)-2-phenyl-3-(2-trifluoromethoxybenzyl)]aminopiperidine; (2S,3S)-3-(5-carbomethoxy-2-methoxybenzyl)amino-2-phenylpiperidine; cis-3-((3,5-dimethylphenyl)methyloxy)-2-phenylpiperidine; or a pharmaceutically acceptable salt thereof.
 13. A method according to claim 1 wherein the tachykinin antagonist is (2S,3S)-3-(2-methoxy-5-trifluoromethoxybenzyl)amino-2-phenylpiperidine or a pharmaceutically acceptable salt thereof. 